Bougie including a light source for performing gastroplasty

ABSTRACT

A gastroplasty method involves a staple line that terminates prior to reaching the gastroesophageal junction such that the bypassed portion of the stomach does not require resection. Additionally, bougies are taught that assist a physician in following the improved staple line of the present invention.

PRIORITY CLAIM TO RELATED APPLICATIONS

This application is a continuation of and claims priority to U.S. patentapplication Ser. No. 14/174,802, entitled Method and “Devices forPerforming Gastroplasty, filed Feb. 6, 2014, which application is acontinuation of and claims priority to U.S. patent application Ser. No.12/865,709, filed Feb. 28, 2011, entitled Methods And Devices ForPerforming Gastroplasty, now U.S. Pat. No. 8,663,149, issued Mar. 4,2014, which is the U.S. National Phase of and claims priority toInternational Patent Application No. PCT/US2009/032741, InternationalFiling Date Jan. 30, 2009, entitled Methods And Devices For PerformingGastroplasty, which claims priority to U.S. Provisional PatentApplication Ser. No. 61/025,619, filed Feb. 1, 2008 by Gagner et al.,entitled Methods And Devices For Performing Gastroplasty, the contentsof all of which are incorporated herein in their entireties.

BACKGROUND OF THE INVENTION

The present invention relates generally to improved methods and devicesfor anchoring a gastroenterologic sleeve within the stomach withoutreliance on sutures, staples, or other mechanisms that puncture thestomach wall. In addition to leaving the stomach walls free ofpunctures, the anchoring system of the present invention preventsmovement of the sleeve in both directions, thereby preventing the sleevefrom being passed through the digestive system but also from refluxingup the esophagus.

According to the Center for Disease Control (CDC), sixty six percent ofAmerican are overweight, and thirty two percent are obese, presenting anoverwhelming health problem. From an economic standpoint, it isestimated that more than 100 billion dollars are spent on obesity andtreating its major co-morbidities. This figure does not includepsychological and social costs. Many health care experts considerobesity the largest health problem facing westernized societies andconsidered obesity an epidemic. From a medical standpoint, obesity isthe primary risk factor for type 2 diabetes and obstructive sleep apnea.It increases the chances for heart disease, pulmonary disease,infertility, osteoarthritis, cholecystitis and several major cancers,including breast and colon cancers. Despite these alarming facts,treatment options for obesity remain limited.

Treatment options include dietary modification, very low-calorie liquiddiets, pharmaceutical agents, counseling, exercise programs and surgery.Diet and exercise plans often fail because most individuals do not havethe discipline to adhere to such plans. When diet and exercise fail,many try dietary supplements and drugs or other ingestible preparationspromoted as being capable of suppressing appetite or inducing satiety.In general, these techniques for treating compulsive overeating/obesityhave tended to produce only a temporary effect. The individual usuallybecomes discouraged and/or depressed after the initial rate of weightloss plateaus and further weight loss becomes harder to achieve. Theindividual then typically reverts to the previous behavior of compulsiveovereating.

Surgical procedures that restrict the size of the stomach and/or bypassparts of the intestine are the only remedies that provide lasting weightloss for the majority of morbidly obese individuals. Surgical proceduresfor morbid obesity are becoming more common based on long-termsuccessful weight loss result.

Bariatric surgery is a treatment for morbid obesity that involvesalteration of a patient's digestive tract to encourage weight loss andto help maintain normal weight. Known bariatric surgery proceduresinclude jejuno-ileal bypass, jejuno-colic shunt, biliopancreaticdiversion, gastric bypass, Roux-en-Y gastric bypass, gastroplasty,gastric banding, vertical banded gastroplasty, and silastic ringgastroplasty. A more complete history of bariatric surgery can be foundon the website of the American Society for Bariatric Surgery athttp://www.asbs.org, the contents of which are incorporated by referenceherein in their entirety.

Advances in laparoscopic surgery have allowed physicians to performoperations that previously required an invasive and painful accessincision to be made. For example, in the case of a sleeve gastrectomy, asurgeon would make an abdominal incision, typically 5 cm or more inlength, which provided access to the abdominal cavity. The surgeon wouldthen suture the stomach together, forming a stoma, using a bougie as aguide along the lesser curvature of the stomach. A bougie is arelatively simple, solid tube inserted into the stomach via theesophagus. The surgeon sutures the stomach shut around the bougie, suchthat the stoma formed matches the size and the narrow, tubular shape ofthe bougie.

Conducting this surgery laparoscopically minimizes trauma to the patientbecause the large abdominal incision is avoided. In female patients, thevagina may be used as an entry point, further minimizing trauma to theabdomen. Recovery time and the chances for infection are greatly reducedusing laparoscopic surgery.

However, laparoscopic surgery adds certain complications. In the case ofa sleeve gastrectomy, because the suture line extends along the entirelength of the stomach, a majority of the stomach is completely isolatedfrom the digestive path. This stomach portion must be removed from thebody. Hence, a sleeve gastrectomy begins with the transection of theshort gastric arteries to the left diaphragmatic crus. Care must betaken to avoid damaging the spleen or its vessels. This makes removal ofthe unused stomach portion the most complicated aspect of a sleevegastrectomy, whether performed laparoscopically or surgically.Laparoscopically transecting these arteries and removing the unusedstomach portion is significantly more difficult than doing sosurgically. In the case of a vaginal-entry laparoscopy, removing theresected stomach portion through the entry opening in the vagina can beparticularly difficult, especially considering that the typical patientundergoing such a surgery as a significantly enlarged stomach.

There is an apparent need for a device and method of performing a sleevegastrectomy obviates the need for removing any portion of the stomach.If the entire stomach can be left in place, patient recovery time,procedural complexity, and patient morbidity rates will be greatlyreduced.

SUMMARY OF THE INVENTION

The present invention provides a device and method for performing asleeve gastrectomy while obviating the need to resect the bypassedportion of the stomach. The need for resection is obviated by endingsuture line a relatively short distance from the gastroesophagealjunction. By leaving this small opening between the stoma and thebypassed portion of the stomach, the bypassed portion can remain inplace without complication, despite the absence of food.

To prevent food from passing through this opening, the suture line isangled away from the gastroesophageal junction near the top of thestomach. This is effected by the use of an embodiment of a bougie of thepresent invention. The bougie includes an extension that, when opened,gives the bougie a Y shape. The resulting stoma has an open top near thegastroesophageal junction but, due to the extension, it is funnel-shapedand thus directs food into the stoma instead of the bypassed stomach.Several embodiments of bougies are described herein.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is an elevation of a first step of the method of the presentinvention;

FIG. 2 is an elevation of a second step of the method of the presentinvention;

FIG. 3 is an elevation of a third step of the method of the presentinvention;

FIG. 4 is an elevation of a fourth step of the method of the presentinvention;

FIG. 5 is an elevation of stomach having undergone the method of thepresent invention;

FIG. 6 is a perspective view of an embodiment of a device of the presentinvention; and,

FIG. 7 is a perspective view of an embodiment of a device of the presentinvention.

DETAILED DESCRIPTION OF THE INVENTION

The present invention includes a method and devices for performing agastroplasty procedure. FIGS. 1-5 show a series of diagrams detailingthe various steps of the method. FIGS. 6-7 depict several embodiments ofvarious devices. By explaining the method first, the various embodimentsof devices will be more easily understood.

The gastroplasty method of the present invention begins by introducing abougie 10 into the stomach A via the esophagus B. The bougie 10 ispreferably shaped to follow the lesser curve C of the stomach A.

Once the bougie 10 is in place such that its distal end 12 is near thegastroduodenal junction D, an extension 14 of the bougie 10 is splayedopen as depicted in FIG. 2. The extension 14 opens enough such that theinner edge 15 of the bougie 10, opposite the lesser curve C, extendsaway from the gastroesophageal junction E.

Next, as seen in FIG. 3, a staple line 16 is followed along the inneredge 15 of the bougie 10 beginning at the bottom of the stomach A andworking up toward the esophagus B. Optionally, suction may be applied tothe stomach A, such that the stomach A collapses and is sucked againstthe bougie 10, making the bougie 10 and the desired staple line 16easier to visualize and follow. Additionally or alternatively, thebougie 10 may include a light source visible through the wall of thestomach A, thereby improving visibility. As seen in FIG. 4, the sutureline 16 will likely include a bend 17 or angle that follows the bougie10.

FIG. 5 shows that the suture line 16 ends prior to reaching the top ofthe stomach. A space 19 is left that allows some communication betweenthe bypassed portion of the stomach F and the newly formed stoma G.After the staple line 16 is complete, the extension 14 is closed againstthe bougie 10 and the bougie 10 is retracted through the esophagus B.

Turning now to FIGS. 6-7, there are shown several embodiments of bougiessuitable for use with the method of the present invention.

FIG. 6 shows a bougie 20 with an extension 22 and an activation device24. The extension 22 is biased shut but is flexible enough to be heldopen using the activation device 24.

The activation device 24 includes a sliding ring 26 that passes aroundthe outside of the bougie 20 but not including the extension 22. Anextending wire 28 passes through an internal lumen of the bougie 20 andexits the bougie through a port 30 located distally of a distal end 32of the extension 22. The extending wire 28 is then routed proximally andattached to the sliding ring 26. Preferably, though not shown in thefigures, a second extending wire is similarly routed on an opposite sideof the bougie 20 such that when pulled, and equal force is applied toboth sides of the ring 26, thereby preventing the ring from hanging upon the bougie 20.

One or preferably two (one shown) retraction wires 34 are also routedthrough an internal lumen of the bougie, exiting at a port 36 locatedproximally of the proximal end 38 of the bougie 20. The retraction wires34 are also connected to the sliding ring 26.

In operation, the bougie 20 is placed as desired in the stomach and theextension 22 is splayed open by pulling on the extending wire or wires28, thereby pulling the ring 26 down in a distal direction. The ring 26is wedged between the extension 22 and the rest of the bougie 20. Thefurther the ring 26 is pulled toward the junction between the extension22 and the bougie 20, the greater the angle between the two becomes.

When the extension 22 is splayed a desired amount, the stapling step ofthe procedure is accomplished. To remove the bougie 20, the retractionwire or wires 34 are pulled, thereby pulling the sliding ring 26 in aproximal direction. The resilient nature of the extension 22 brings itflush against the bougie 20 and the bougie 20 may be removed.

Turning now to FIG. 7, there is shown another embodiment of a bougie 40of the present invention with an extension 42 and an activation device44. The extension 42 is biased open but is flexible enough to be heldclosed using the activation device 44.

The activation device 44 includes a sliding ring 46 that passes aroundthe outside of the bougie 40, including the extension 42. An extendingwire 48 passes through an internal lumen of the bougie 40 and exits thebougie through a port 50 located near or distally of a distal end 52 ofthe extension 42. The extending wire 48 is then routed proximally andattached to the sliding ring 46. Preferably, though not shown in thefigures, a second extending wire is similarly routed on an opposite sideof the bougie 40 such that when pulled, and equal force is applied toboth sides of the ring 46, thereby preventing the ring from hanging upon the bougie 40.

One or preferably two (one shown) retraction wires 54 are also routedthrough an internal lumen of the bougie, exiting at a port 56 locatedproximally of the proximal end 58 of the bougie 40. The retraction wires54 are also connected to the sliding ring 46.

In operation, the bougie 40 is placed as desired in the stomach and theextension 42 is splayed open by pulling on the extending wire or wires48, thereby pulling the ring 26 down in a distal direction. The ring 46releases the extension 42 and the biased-open extension is free tosplay. Depending on the how over-sized the ring 46 is compared to thebougie, the further the ring 46 is pulled toward the junction betweenthe extension 42 and the bougie 40, the greater the angle between thetwo becomes.

When the extension 42 is splayed a desired amount, the stapling step ofthe procedure is accomplished. To remove the bougie 40, the retractionwire or wires 54 are pulled, thereby pulling the sliding ring 46 in aproximal direction. The ring 46 collapses the extension 42 flush againstthe bougie 40 and the bougie 40 may be removed. Preferably the port 56is located such that the ring 46 cannot be drawn past the proximal endof the extension 42, such that an accidental splaying of the extension42 during withdrawal is not possible.

Although the invention has been described in terms of particularembodiments and applications, one of ordinary skill in the art, in lightof this teaching, can generate additional embodiments and modificationswithout departing from the spirit of or exceeding the scope of theclaimed invention. For example, one skilled in the art will realizeseveral embodiments bougies that include an extension and various was todeploy and retract this extension. Just a few, non-limiting examples ofother devices include, but are not limited to, screw-activated devices,balloon activated devices, ratcheting devices, and the like.Accordingly, it is to be understood that the drawings and descriptionsherein are proffered by way of example to facilitate comprehension ofthe invention and should not be construed to limit the scope thereof.

We claim:
 1. A bougie for use in performing a gastroplasty, the bougiecomprising: an elongate body having a segment configured to enter astomach of a patient, the segment being shaped to follow a lesser curveof the stomach; an extension member having a proximal portion connectedto the segment of the elongate body, the extension member being movablefrom a retracted position in which the extension member is generallyaligned with the elongate body, to an extended position in which theextension member extends at an angle away from the segment within thestomach for positioning a distal portion of the extension member awayfrom a gastroesophageal junction of the stomach; an activation mechanismthat is configured to move the extension member from the retractedposition to the extended position; and an actionable light sourceprovided to assist, when activated, in the establishing of a junctionline along which opposed walls of the stomach are joinable.
 2. Thebougie of claim 1, wherein the distal portion of the extension member isa free-end that is spaced-away from the segment to define a Y-shape whenthe extension member is in the extended position.
 3. The bougie of claim1, wherein the activation mechanism comprises at least one extendingwire which, when manipulated from outside of the stomach, moves theextension member to the extended position.
 4. The bougie of claim 1,wherein the activation mechanism comprises at least one retracting wirewhich, when manipulated from outside of the stomach, moves the extensionmember to the retracted position.
 5. The bougie of claim 1, wherein theactivation mechanism comprises a ring slidable along the extensionmember and biasing the extension member in the extended position whenplaced nearby the proximal portion of the extension member.
 6. Thebougie of claim 1, wherein the activation mechanism comprises a ringslidable along the extension member and biasing the extension member inthe retracted position when placed nearby the distal portion of theextension member.
 7. A bougie for use in performing a gastroplasty, thebougie comprising: an elongate body having a segment configured to entera stomach of a patient; an extension member connected to the elongatebody and being movable from a retracted position in which the extensionmember is generally aligned with the elongate body, to an extendedposition in which a section of the extension member extends at an angleaway from the elongate body within the stomach, thereby establishing ajunction line along which opposed walls of the stomach are joinable; anactivation mechanism that is configured to move the extension memberfrom the retracted position to the extended position; and an actionablelight source provided to assist, when activated, to establish thejunction line.
 8. The bougie of claim 7, wherein the extension memberhas a proximal portion and a distal portion and the segment of theelongate body has a forward portion, an intermediate portion and arearward portion, wherein the proximal portion of the extension memberis connected to the intermediate portion of the segment.
 9. The bougieof claim 8, wherein the elongate body and the extension member areconfigured such that, in the extended position, the extension member andthe forward portion of the segment define the junction line.
 10. Thebougie of claim 8, wherein the distal portion of the extension member isa free-end that is spaced-away from the rearward portion of the segmentin the extended position.
 11. The bougie of claim 10, wherein thefree-end is rounded.
 12. The bougie of claim 10, wherein the extensionmember is generally straight.
 13. The bougie of claim 7, wherein theelongate body and the extension member are configured such that, in theretracted position, the extension member lies against part of theelongate body.
 14. The bougie of claim 7, wherein the segment of theelongate body is shaped to follow a lesser curve of the stomach.
 15. Thebougie of claim 7, wherein the activation mechanism is configured toposition the section of the extension member at different anglesrelative to the elongate body.
 16. The bougie of claim 7, wherein theactivation mechanism is configured to position the section of theextension member at an angle away from a gastroesophageal junction ofthe stomach in the extended position.
 17. The bougie of claim 7, whereinthe activation mechanism comprises at least one wire coupled to theextension member for selectively moving said extension member betweenthe retracted position and the extended position.
 18. The bougie ofclaim 7, wherein the activation mechanism comprises a biasing membercooperating with the extension member to bias the extension member inthe retracted position or in the extended position.
 19. The bougie ofclaim 7, wherein the activation mechanism comprises a ring slidablealong the extension member for biasing the section of the extensionmember at the angle away from the elongate body.
 20. The bougie of claim7, wherein the extension member has a generally C-shaped cross-section.